DeAnn Prettyman (C) A.S.C.P, ICP-APO

Experience

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  Boyce and Bynum Pathology Labs

  Oct 2004 - May 2009

  Lab Tech II

  Processed specimens and performed various lab procedures in both hematology and chemistryResponsible for daily maintenance and quality control of Chemistry and Hematology analyzers.Gained valuable laboratory knowledge while working in a fast-paced environment

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  Encompass Medical Group

  May 2009 - Mar 2012

  Lead Medical Laboratory Tech

  Performs routine laboratory analyses to ensure 100% accuracy and precision.Responsible for regular maintenance and quality control to ensure proper instrumentation.In control of weekly inventory, stocking of reagents, controls, and calibrators, along with monitoring current lots to ensure complete laboratory compliance. Provides assistance to Lab Manager to ensure compliance to all COLA practices and proceduresProficient in phlebotomyExperienced in data entry including LabDaq LIS and Centricity GE EMR systems.Maintains superior customer service while working with doctors and patients.Held accountable for training and orientation of all new employees. Show less

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  Heritage Labs/Clinical Reference Laboratory

  Mar 2012 - Dec 2014

  Med Tech

  Oversaw daily processes in the Urine Chemistry department, including analysis of drugs of abuse and regular testing, to ensure correct and error free client resultsCompleted routine maintenance of Chemistry analyzers to uphold streamlined performanceEnsured complete compliance for all CAP and CLIA procedures Controlled monthly inventory, stocking of reagents, controls, and calibrators, along with monitoring current lots to ensure complete laboratory complianceExperienced in Roche COBAS 8000 automated instrumentation and software testing Show less

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  Cerner Corporation

  Dec 2014 - Sept 2022

  Responsible for the design and management of all change requests, defects and enhancements from product backlog into epics and user stories. In managing the backlog, I work closely with technical experts to determine release schedules.Create product requirements to ensure all risks, hazards and regulatory needs are evaluated for clients. Utilizing my domain and regulatory knowledge, I manage communication between teams and stakeholders, including our third-party quality clinical decision support mechanism to build functional requirements. Subject matter expert for all workflow, configuration, references and build guides including updating documentation with all releases. I perform knowledge shares and demos for internal and external stakeholders, along with joining client troubleshooting sessions to assist.In addition to creating clear stories and acceptance criteria, I perform and document all functional testing. Any risks are documented along with hazard analysis and possible mitigation.Collaborate with product team to shape roadmap by recognizing opportunities for improvement within processes and development. This includes the long-term roadmap or just a single sprint. Show less

  • Senior Product Owner

    Mar 2021 - Sept 2022

  • Senior Solution Designer

    Apr 2020 - Sept 2022

  • Solution Designer, Clinical Terminologist

    Dec 2014 - Apr 2020
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  The St. John Group

  Sept 2022 - now

  Consultant - Project Manager

  Project Manager for Association of Public Health Laboratories (APHL) to lead interoperability between PHLs, PHAs for data exchange. In this role, I oversee the upgrade of the PHLIP HL7 2.5.1 message for public health laboratories for more efficient communication to stakeholders. In addition, managing the day-to-day scheduling and project planning for the implementation of new assays to the PHLIP feed for surveillance purposes while identifying and mitigating risks. I fulfill project needs that are necessary for the scope and roadmap while working with multiple stakeholders. Show less